Numan Muhammad, Alouffi Abdulaziz, Almutairi Mashal M, Tanaka Tetsuya, Ahmed Haroon, Akbar Haroon, Rashid Muhammad Imran, Tsai Kun-Hsien, Ali Abid
Department of Zoology, Abdul Wali Khan University Mardan, Mardan 23200, Pakistan.
King Abdulaziz City for Science and Technology, Riyadh 12354, Saudi Arabia.
Animals (Basel). 2023 Oct 17;13(20):3232. doi: 10.3390/ani13203232.
ticks transmit and species to a wide range of animals. The spreading of ticks and tick-borne pathogens has been attributed to transhumant herds, and research on these uninvestigated issues has been neglected in many countries, including Pakistan. Recently, we used internal transcribed spacer (ITS) and 16S ribosomal DNA partial sequences to genetically characterize ticks and their associated spp. However, the data on its sequence and associated spp. and spp. are missing. This study aimed to genetically characterize based on the sequence and their associated spp. and spp. The ticks were collected from small ruminants: sheep () and goats () of transhumant herds in district Shangla, Dir Upper and Chitral, Khyber Pakhtunkhwa (KP), Pakistan. Out of 129 examined hosts, 94 (72.87%) (56 sheep and 38 goats) were infested by 352 ticks, including adult females (175; 49.7%) followed by nymphs (115; 32.7%) and males (62; 17.6%). For molecular analyses, 121 ticks were subjected to DNA isolation and PCR for the amplification of the sequence for , 18S rDNA for spp. and 16S rDNA sequences for spp. The obtained sequence showed 89.29%, 88.78%, and 88.71% identity with and , respectively. Phylogenetically, the present sequence clustered with the complex. Additionally, the 18S rDNA sequence showed 98.11% maximum identity with cf. and 97.99% identity with . Phylogenetically, spp. clustered with the cf. and . In the case of spp., the 16S rDNA sequence showed 100% identity with and phylogenetically clustered with the . PCR-based DNA detection targeting the amplification of and sequences of spp. and spp., respectively, was unsuccessful. This is the first phylogenetic report based on and new locality records of , and the associated -like and . Significant tick surveillance studies are needed in order to determine the epidemiology of ticks and their associated pathogens.
蜱虫会将病原体传播给多种动物。蜱虫及其传播的病原体的扩散被认为与游牧畜群有关,而包括巴基斯坦在内的许多国家都忽视了对这些未被研究的问题的研究。最近,我们利用内转录间隔区(ITS)和16S核糖体DNA部分序列对蜱虫及其相关的物种进行了基因特征分析。然而,关于其序列以及相关物种的数据缺失。本研究旨在基于该序列及其相关的物种对蜱虫进行基因特征分析。这些蜱虫采自巴基斯坦开伯尔-普赫图赫瓦省(KP)尚拉县、上迪尔县和奇特拉尔县游牧畜群中的小反刍动物:绵羊()和山羊()。在129只被检查的宿主中,94只(72.87%)(56只绵羊和38只山羊)被352只蜱虫寄生,其中成年雌性蜱虫(175只;49.7%)最多,其次是若虫(115只;32.7%)和雄性蜱虫(62只;17.6%)。为了进行分子分析,对121只蜱虫进行了DNA提取和PCR,以扩增该蜱虫的序列、用于物种分析的18S rDNA以及用于物种分析的16S rDNA序列。获得的该蜱虫序列与和分别显示出89.29%、88.78%和88.71%的同一性。在系统发育上,目前的该蜱虫序列与复合体聚集在一起。此外,18S rDNA序列与cf.显示出98.11%的最大同一性,与显示出97.99%的同一性。在系统发育上,物种与cf.和聚集在一起。在物种的情况下,16S rDNA序列与显示出100%的同一性,并在系统发育上与聚集在一起。分别针对物种和物种的序列扩增进行基于PCR的DNA检测未成功。这是基于该蜱虫以及新的地理记录以及相关的类似物种和物种的第一份系统发育报告。为了确定该蜱虫及其相关病原体的流行病学,需要进行重要的蜱虫监测研究。